US8420557B2 - Polyethylene-based, soft nonwoven fabric - Google Patents

Polyethylene-based, soft nonwoven fabric Download PDF

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Publication number
US8420557B2
US8420557B2 US11/425,340 US42534006A US8420557B2 US 8420557 B2 US8420557 B2 US 8420557B2 US 42534006 A US42534006 A US 42534006A US 8420557 B2 US8420557 B2 US 8420557B2
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nonwoven fabric
fibers
polyethylene
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US20070134478A1 (en
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Markus Haberer
Henning Röttger
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Fitesa Germany GmbH
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Fiberweb Corovin GmbH
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Priority to US12/363,912 priority patent/US20090136606A1/en
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    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D4/00—Spinnerette packs; Cleaning thereof
    • D01D4/02—Spinnerettes
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/08—Melt spinning methods
    • D01D5/098—Melt spinning methods with simultaneous stretching
    • D01D5/0985—Melt spinning methods with simultaneous stretching by means of a flowing gas (e.g. melt-blowing)
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/06—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/005—Synthetic yarns or filaments
    • D04H3/007—Addition polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/608—Including strand or fiber material which is of specific structural definition
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
    • Y10T442/641—Sheath-core multicomponent strand or fiber material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/681—Spun-bonded nonwoven fabric
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/69—Autogenously bonded nonwoven fabric

Definitions

  • the present invention concerns a nonwoven fabric the fibers of which have a polyethylene at least on their surface, with the fibers being thermally bonded. Furthermore claimed is a device for the manufacture of a nonwoven fabric using a polyethylene-containing polymer, and a procedure for the manufacture of a nonwoven fabric the fibers of which have polyethylene at least on part of their surface.
  • nonwoven fabrics have the most varied applications. Because of their multiple influence parameters, these properties can often be determined only by means of elaborate tests, where in addition to the effects of the polymer material used, also machine effects, ambient conditions and other parameters have to be taken into account.
  • a nonwoven fabric is obtained from WO 02/31245 A2 that presumably is particularly soft.
  • a nonwoven fabric is obtained based on multiple experimental parameters that are supposedly manufactured with a consolidation surface area of at least 30% of the nonwoven fabric surface area and an abrasion coefficient of less than 0.30 mg/cm 2 .
  • a pre-consolidated nonwoven fabric is passed though a first and then a second calender, where thermal bonding takes place in both calenders. In a calender placed downstream, the material thus doubly consolidated is stretched essentially in CD direction, before being spooled and transported for further processing.
  • Certain embodiments of the present invention satisfy at least some of the aforementioned tasks by providing a soft yet robust nonwoven fabric.
  • a nonwoven fabric is proposed the fibers of which have a polyethylene at least on the surface, where the fibers are bonded and the nonwoven fabric has an abrasion rate less than 0.8 mg/cm 2 .
  • the fibers preferably consist essentially of polyethylene.
  • the nonwoven fabric is preferably thermally bonded only once.
  • the nonwoven fabric has an abrasion resistance rate less than 0.2 mg/cm 2 , especially in the range between 0.2 to 0.09 mg/cm 2 .
  • a further implementation comprises a nonwoven fabric with a consolidation area fraction of less than 0.2 mg/cm 2 , especially less than 32%, preferably less than 28% a preferred embodiment comprises a nonwoven fabric with an abrasion rate of less than 0.3 mg/cm 2 and a consolidation area fraction of less than 30%.
  • the nonwoven fabric fibers have polyethylene at least on their surface, where the fibers are thermally bonded and the nonwoven fabric shows an abrasion of less than 0.5 mg/cm 2 , in particular of less than 0.4 mg/cm 2 , and an consolidated surface fraction of less than 23%, in particular of less than 20%.
  • a nonwoven fabric can be manufactured with an abrasion of less than 0.3 mg/cm 2 , preferably even of less than 0.2 mg/cm 2 and in particular, of less than 0.1 mg/cm 2 . It is also possible to keep the consolidated area fraction to below 16%.
  • the abrasion is here determined as follows:
  • the abrasion is determined using a Sutherland Inc. Rub Tester, a standard instrument in the paper industry. This instrument can for instance be obtained from the Richard Schmitt Company, In der Einsteinstrasse 20, 64668 Rimbach. The Tester is described in principle also in U.S. Pat. No. 2,734,375.
  • the measurement principle provides that a surface of the nonwoven fabric be treated with sandpaper under defined conditions and the abrasion is determined gravimetrically.
  • Abrasion is here defined as follows: the gravimetrically determined mass of loose fiber per unit surface area [mg/cm 2 ].
  • a Sutherland Inc. Rub Tester with a 1 kg bearing load (AGS) is required, with a holder for the sandpaper, an analytical balance with a precision of ⁇ 0.0001 g, a dinking die and stamp press, and a 2 kg hand roller.
  • AGS 1 kg bearing load
  • Sandpaper (aluminum oxide), 320 grain, width 50.8 mm; double-side adhesive tape, from 3M, Article No. 9195, hereinafter called Tape 1; to collect the fibers, an adhesive tape, from 3M, Article No. 3126c, hereinafter called Tape 2; silicone paper; metal sheets to glue on the nonwoven fabric.
  • Sample preparation is performed before carrying out the test. To this end a piece of nonwoven fabric of size 20 cm ⁇ 5 cm is punched out using a dinking die. Care must be taken to verify whether the nonwoven fabric is tested in the production direction (MD), or in the direction perpendicular to the production direction (CD). Thus, if the nonwoven fabric sample is to be tested in MD, then the MD must be oriented parallel to the longer side of the nonwoven fabric specimen. The test report must indicate whether the test was performed in MD or CD. When handling the nonwoven fabric specimen, care must be taken not to touch it with bare hands, to avoid surface contamination. Tape 1 has adhesive sides that adhere with different strengths. The more strongly adhering side is the side that remains covered when the tape is let out.
  • the nonwoven fabric must be glued onto this side.
  • the side that is uncovered during the unwinding of Tape 1 must be covered with silicone paper and the tape cut into 15 cm long pieces.
  • the silicone paper from the more strongly adhering side of Tape 1 is removed and the nonwoven fabric is glued onto tape 1 on the side not to be tested.
  • the nonwoven fabric has two sides: a smooth and an consolidated side. Hence different abrasion values can be determined for the same nonwoven fabric, depending on the side tested.
  • the test is performed in the following steps:
  • the Sutherland Inc. Rubb Tester is set to 20 test cycles, selecting velocity step 1 on the instrument. This corresponds to 42 cycles per minute.
  • a 20 cm long piece of sandpaper is cut.
  • the sandpaper is attached to the AGS of the Sutherland Inc. Rubb Tester, in such a way that the sandpaper no longer moves. Note that a new piece of sandpaper must be used for each test.
  • the removable paper is peeled off the second side of tape 1 and the composite of tape 1 and the nonwoven fabric is glued onto the metal sheet provided for that purpose. The composite must be glued precisely in the marked area on the metal sheet.
  • the nonwoven fabric is then rolled over twice with the 2 kg hand roller. No additional force is to be applied.
  • the weight of the metal sheet and the tape 1/nonwoven fabric composite is then determined on an analytical balance to four decimal places, and recorded (G1).
  • the AGS is then hung into the mounting support on the Sutherland Inc. Rubb Tester. Care must be taken here that the surface of the nonwoven fabric to be tested is not damaged and no unnecessary pressure is applied to it. Once the measurement has been performed, the AGS is carefully removed. Then a 20 cm long strip of tape 2 is cut and placed loosely on the specimen. Care must be taken that the adhesive side of tape 2 is not touched with bare hands. Next pass the 2 kg hand roller once over the glued-on tape 2. No additional force is applied here. Next tape 2 is pulled off the surface of the nonwoven fabric specimen. The nonwoven fabric is weighed precisely with the sample holder, to ⁇ 0.0001 g accuracy. The weight so determined is recorded as “overall nonwoven fabric weight” (G2).
  • results will differ depending on whether the smooth or the consolidated side of the nonwoven fabric is examined. Differences can also arise if the sample is tested once in MD and another time in CD orientation. To obtain uniform measurement results, care must be taken that the test conditions are uniform. In multiple determinations of an abrasion value, the mean value and the standard deviation are calculated. In addition, the minimum and the maximum values are recorded. The measurement precision of the calculated abrasion is reported to three decimal places.
  • the nonwoven fabric shows an abrasion of less than 0.3 mg/cm 2 on the consolidated side.
  • the difference in abrasion between the consolidated and the smooth side is less than 70%. It is in particular preferred that abrasion of the consolidated side amounts to at most 50%, in particular less than 30%, of the abrasion on the smooth side of the nonwoven fabric.
  • the consolidated surface of the nonwoven fabric can serve as outer layer of a product, compared to the smooth side.
  • the reduced abrasion tendency of the material makes it possible to use the nonwoven fabric in particular in applications in which a pronounced tendency to lint formation could lead to undesirable side effects.
  • a nonwoven fabric is made available, with fibers that have polyethylene on their surface, whereby the nonwoven material exhibits a dynamic coefficient of friction (COF: coefficient of friction) of 0.19-0.5.
  • COF coefficient of friction
  • the dynamic coefficient of friction will be of 0.25-0.35. If the nonwoven fabric has a coefficient of friction in this range, then it can be successfully used wherever it is important to use the nonwoven fabric without a high abrasion effect.
  • the dynamic coefficient of friction CoF is determined using a measurement principle in which a sled is covered with a nonwoven fabric sample and then pulled in a defined manner over a level area also covered with the same nonwoven fabric. The intervening forces are recorded by a tensile tester.
  • the standard to be consulted here is TEFO method 18-66.
  • the dynamic coefficient of friction is thus dimensionless.
  • the F stoff used is the mean force in Newton obtained by the measurement.
  • the value W indicates the weight of the nonwoven fabric specimen W Vlies wrapped around the sled, added to the weight of the sled W Schlitten .
  • the weight of the sled is 195.3 g.
  • the concept “friction body” is defined as “sled with attached nonwoven fabric sample” and the concept “friction table” is defined as “platform with applied nonwoven fabric”.
  • a tensile tester for instance a Zwick 2.5—is required to perform the test method, as well as a sled with a nylon thread and an adapter for the test machine, a platform with a turn pulley and a balance.
  • the specimen to be tested is prepared as follows: a nonwoven fabric specimen 1 is cut to size 65 ⁇ 100 mm and a second nonwoven fabric 2, to size 140 ⁇ 285 mm. Care must be taken here that the long sides are cut either in MD or CD alignment. While carrying out the test method, the platform is attached to the tensile tester. A 100 N load cell is installed in the tensile tester. Next the nonwoven fabric specimen 1 is weighed to 0.001 g precision and the weight W Viles is recorded.
  • the nonwoven fabric specimen 1 is cut centrally on one of the narrow sides, to a depth of 3 cm and attached to the sled using adhesive tape. Care must be taken that the adhesive tape is not on the friction side of the nonwoven fabric specimen. Furthermore, care must be taken that the orientation of the nonwoven fabric is observed, i.e., its smooth or its consolidated side are indicated. In a subsequent evaluation, care must be taken to indicate which side was used in the test.
  • the nonwoven fabric specimen 2 is attached to the platform using a double-sided adhesive tape. Care must be taken here too that the adhesive tape is not in the friction area of the nonwoven fabric specimen.
  • the nonwoven fabric specimen must lie wrinkle-free on the platform, with the longer side parallel to the longer side of the platform. Here too, in the subsequent evaluation care must be taken to know what orientation—smooth or consolidated side—the nonwoven fabric presented.
  • the measurement at the tensile tester can then begin and the friction body can slide over the friction table.
  • the mean force F kar and the coefficient of friction are determined for each specimen.
  • the force measured is determined to a precision of 0.01 N, with the calculated dynamic coefficient of friction being indicated with two decimal places.
  • a nonwoven fabric is provided with fibers that have polyethylene at least on their surface, where the nonwoven fabric has a bending stiffness in MD direction in the range of 0.03-0.23 mN/cm and in CD direction in the range of 0.01-0.15 mN/cm.
  • the softness of the nonwoven fabric can for instance be influenced via the bending stiffness. It has proven to be advantageous for the nonwoven fabric to have a minimum and a maximum bending stiffness, since for instance in the use of the nonwoven fabric in contour matching, as in medical and hygiene articles, too stiff a material would be undesirable.
  • nonwoven fabric to have fibers with a titer below 3 dtex, in particular below 2.8 dtex. This is an additional way to influence abrasion.
  • another property such as permeability for liquids and/or gases, can be affected hereby.
  • the nonwoven fabric preferably has a tensile force at maximum peak in CD direction of at least 3 N, preferably of at least 8 N, in particular 12 N, and in MD direction of at least 5 N, in particular of at least 10 N, preferably of at least 15N.
  • the nonwoven fabric has a tensile force in CD direction at least 20 N high and in MD direction at least 25 N high.
  • the tensile force is here determined following DIN/EN 29073-3, June 1992 version. However, the following deviation is adopted in the determination: the distance between the clamps is 100 mm, instead of 200 mm, as the standard states.
  • the velocity at which a cross-head of the measurement machine is moved is of 200 mm/min, instead of 100 mm/min as defined in the standard.
  • the specimen size is 50 mm in width and 200 mm in length.
  • care must be taken that the tension acting on the nonwoven fabric lies between 0 and 0.5N.
  • the test is performed until the specimen tears. From the force-elongation curve so determined it is possible to determine the maximum tensile force at maximum peak and therewith the elongation at maximum force in %, the elongation at 5 N and at 10 N in % and the tensile force at 5% elongation, in Newton.
  • the tensile force is determined with a precision of 0.1 N and the elongation with a precision of 0.1%.
  • the nonwoven fabric exhibits a grammage of 13-30 gsm. According to another implementation, the grammage has a value of 15-20 gsm. With an appropriate embossing, at such a grammage sufficient tear forces can be made available for applications in particular in the hygiene area.
  • Another implementation provides for a nonwoven fabric with softness that is preferably greater than 2.1.
  • a softness value greater than 3.1 is particularly desired.
  • One implementation provides for at least part of the fibers, preferably all fibers, to have a core-sheath structure.
  • This core-sheath structure is preferably caused by different polymers.
  • the casing can for instance be polyethylene, while the core has polypropylene.
  • polymer mixtures can also be used here, with a core of different composition than the polymer composition of the casing.
  • different polyethylene for the core and for the casing can be used.
  • Another implementation provides for the core-sheath structure to include a light oxidation surface. In particular this oxidation surface can exist additionally. By means of an oxidation surface it is possible to improve the bonding properties in a subsequent thermal bonding step.
  • a polypropylene has an oxidation layer on its surface.
  • the core-sheath structure can be such that for instance a multi-component material is present, in particular a two-component material, where the casing is not arranged homogeneously but inhomogeneously around the core.
  • the arrangement can for instance be in the form of thickenings and thickness reductions.
  • the casing arrangement can even be partially discontinuous, so that the core appears in at least some segments.
  • the core-sheath structure in the form of a two-component fiber, can also be eccentric. Segment fibers can also be formed.
  • a further implementation provides for at least part of the fibers to have a non-circular cross-section.
  • the fiber cross-section can be oval, flattened, trilobal or in any form that increases the surface. Besides an especially large surface area, in this manner a deposit on the fiber surface can achieve better adherence, because of the enlarged surface.
  • the fiber can preferably have a star-shaped cross-section, where a gusset is formed between two radially outward stretching segments. An active substance can for instance be placed in this gusset.
  • the fiber can be at least either partially or completely equipped with an additional covering.
  • This covering can be applied on the entire surface of the nonwoven fabric.
  • foam depositions, spray depositions, wetting procedures, vapor deposition procedures, ionization procedures and/or immersion bath procedures, as well as other possibilities can be used.
  • the covering can be applied off-line or on-line.
  • At least a part of the nonwoven fabric fibers can have a hollow core.
  • a hollow core can for instance make available an improved liquid uptake.
  • the hollow core can also contain an active agent that is gradually released to the outside.
  • a further development provides for at least a part of the fibers, in particular all fibers of the nonwoven fabric, to be curled.
  • a curl can for instance be achieved by means of special heat treatments, making use of different polymers contained in a nonwoven fabric fiber. Curling can also be achieved by stretching the nonwoven fabric or respectively, its fibers.
  • the curling is accomplished by means of a process step before, during and/or after a consolidation process, in particular a thermal bonding process to bond the nonwoven fabric fibers to each other.
  • a process step before, during and/or after a consolidation process, in particular a thermal bonding process to bond the nonwoven fabric fibers to each other.
  • the nonwoven fabric provides for the nonwoven fabric to be a thermally bonded spunbonded nonwoven fabric.
  • Another implementation provides for the nonwoven fabric to be a carded nonwoven fabric.
  • a device for the manufacture of a nonwoven fabric using a polyethylene-containing polymer, with a take-down mechanism that causes the take-down of the polyethylene beneath a spinning plate, where the spinning plate has an L/D ratio of 4-9.
  • L refers to the length of spinning plate boring through which the polymer flows to form a thread upon exiting.
  • D in turn indicates the diameter of the spinning plate boring.
  • the boring can be manufactured by different processes.
  • the L/D ratio is between 6 and 8.
  • Yet another implementation provides for the L/D ratio to be between 4 and 6.
  • the L/D ratio is in between 4.5 and 9, especially between 5.5 and 7.5.
  • the spinning plate temperature—and according to a continued development, also the polymer temperature before it passes through the spinning plate— is coordinated with the L/D ratio, in conjunction with the polymer material.
  • the spinning plate can have different configurations.
  • the diameter D can be uniform over at least most of the length L.
  • “uniform” can mean constant, but also evenly increasing or decreasing.
  • the diameter D can also have a narrowing in its initial range, while being nearly constant in the remaining portion.
  • the length L is preferably such that it represents the shortest distance from one side of the spinning plate to the opposite side.
  • at least part of the spinning plate holes are not at right angles to at least the side of the spinning plate on which they open.
  • Another configuration provides for the neighboring holes in the spinning plate to be arranged in rows parallel to each other along one width and one length of the spinning plate.
  • Another implementation provides for neighboring holes in the spinning plate to be offset with respect to each other. This makes it possible for the polymer threads exiting the spinning plate borings to be exposed to a quenching agent to cool them and so that they can be stretched.
  • the spinning plate geometry and the geometry of spinning plate boring arranged on it can be coordinated with the flow velocity of the quenching agent.
  • an enclosure for a take-down device for the polyethylene and the spinning plate Preferably it is provided an enclosure for a take-down device for the polyethylene and the spinning plate.
  • a take-down device for the polyethylene and the spinning plate Preferably it is provided for such an enclosure to be penetrable, at least in the area of the take-down mechanism.
  • a further development provides for the enclosure to extend at least in part in the direction of a deposition device for the polymer threads. This makes it possible to purposefully reduce environmental influences due to the conditions surrounding the device, and thereby intentionally adjusting the temperature conditioning of the take-down of the polymer threads and thereby, cooling and stretching.
  • the device to have an enclosure, as housing.
  • the enclosure preferably is under a pressure of 10-50 mbar. This allows achieving a particularly good stretching of the polymer threads.
  • at least a one-sided quenching air flow be arranged beneath the spinning plate.
  • a two-sided quenching flow can also be provided.
  • the quenching air can here flow perpendicularly and/or at an angle onto the polymer threads.
  • the quenching air can be temperature conditioned. This means that at least its temperature, but for instance also its moisture content, its velocity and hence its pressure and the volume flow, and/or other parameters, can be intentionally adjusted.
  • a split quenching to be arranged underneath the spinning plate.
  • a first quench airflow quenches the polymer threads and stretches them. It can also be provided for an optimization of the stretching during the first quenching by heating the quenching air, so that the fiber is not cooled too fast and hence can be stretched longer.
  • a subsequent quenching has a differently conditioned quench air, compared to the first. This conditioning is adapted to the prestretched and cooled state of the polymer threads existing at that point. The conditioning can provide for the second quenching to have a higher temperature, higher volume flow, higher flow, higher velocity and/or a different flow direction than the first quenching.
  • the second quenching has lower conditioning parameters than the first.
  • the device preferably has at least two areas, in the zone beneath the spinning plate and to a deposition device, in particular a screen belt, in which different take-down parameters can be set.
  • a quench differing in many ways can also be used for this purpose.
  • the device provides for the device to be such that the take-down velocity can be adjusted in a range of 900-6000 m/min.
  • different procedure parameters, and polymer threads as well as polymer compositions can be processed into a nonwoven fabric.
  • one or several compactors can be provided those are able to realize different take-down velocities.
  • a nozzle system can also be provided to select different take-down velocities.
  • a nozzle geometry can here be adjustably modified.
  • a take-down velocity can also be set via different tempering and pressure settings of a quenching air. This can in particular be realized in conjunction with a changeable or different nozzle geometry.
  • One further development for instance provides for the depressurizing of a pressurized quenching air. Depressurization can be achieved in different ways, so that different take-down velocities can thereby be set.
  • a nozzle arrangement for the flow-through of polymer threads from the spinning plate to be placed under the spinning plate, which first has a constriction, then an averaged diameter and finally, an enlargement.
  • the nozzle arrangement can here be in one or several pieces.
  • the nozzle arrangement can also be subdivided.
  • the nozzle arrangement is penetrable, i.e., it allows screening the polymer threads from the device's immediate surroundings.
  • the nozzle arrangement is such that the polymer threads enter in contact with the immediate surroundings of the device only immediately before they are deposited, for instance on a screen belt. Before that the polymer threads are only under a conditioned state, determined by the quenching air and/or other media supplied to the nozzle arrangement.
  • the spinning plate has furthermore proven to be advantageous for the spinning plate to have at least 4500 holes/m, in particular more than 6000 holes/m and preferably, more than 7000 holes/m.
  • Another implementation provides for the spinning plate to have a hole density of 4.5-6.3 holes/cm 2 .
  • the spinning holes in the spinning plate can hereby have a taper. In this manner it is possible to achieve a nozzle effect and in particular, an acceleration of the polymer material inside the spinning plate. This makes it possible to spin the polymer material into thin polymer threads.
  • the borings in the spinning plate for the flow-through of the polymer is preferably for the borings in the spinning plate for the flow-through of the polymer to have a diameter larger than 0.4 mm.
  • a size makes it possible, on the one hand, to achieve a high throughput of polymer through the spinning plate, while on the other hand with such a size sufficiently fine nonwoven fabric threads can be obtained, preferably of less than 3 dtex, in particular of less than 2.8 dtex.
  • the boring diameter of at least 0.4 mm also makes possible with the polyethylene-containing material to achieve throughputs higher than 100 kg/h/m and especially higher than 120 kg/h/m, in particular of more than 150 kg/h/m and preferably, of higher than 180 kg/h/m.
  • throughputs of polyethylene-containing polymer material can be attained that exceed 200 kg/h/m and that make possible a nonwoven fabric with a titer of less than 3 and an abrasion of less than 0.4 mg/cm 3 at an consolidated area fraction of less than 30%, preferably less than 25%, especially less than 20%.
  • the borings in the spinning plate have a diameter in the range of 0.4-0.7 mm, preferably up to 0.9 mm.
  • the boring diameter is of 0.6-0.9 mm.
  • An improvement in the spinning of polyethylene-containing polymer material can be achieved by a coating on the spinning plate.
  • the coating can for instance be chromium plating. However, it can also be a PTFE treatment. Other coatings that in particular reduce adherence of polymer material, but do not impede heat passage, can also be used.
  • a further implementation provides for the device to include a heatable calender that is connected to the device.
  • the calender preferably has at least a smooth-surfaced roller and an engraved roller.
  • the smooth-surfaced roller and the engraved roller are heated to different extents.
  • the smooth-surfaced roller is at a lower temperature than the engraved roller.
  • Thermal bonding of the nonwoven fabric material is performed with the heatable calender, to set the consolidated area fraction to preferably less than 23% and in particular, to less than 20%, in particular in a range of 13-18%.
  • the thermal bonding step can be additionally furthered by means of a coating on at least one of the calender rollers.
  • the coating is such that adhesion is avoided, in particular adhesion of the polymer material heated in the thermal bonding step.
  • One calender roller can for instance have a PTFE coating.
  • Heating of the calender rollers is preferably accomplished by means of internal heating, for instance ensured by a liquid circulation.
  • a calender roller can also be heated by means of gaseous media.
  • different heating circuits are provided, so that different heating is possible in two opposing calender rollers.
  • a temperature difference of at least 2° C. can be set, in particular a temperature difference of up to 10° C. It is also possible to heat both calender rollers to the same temperature.
  • the device include an arrangement that allows the manufacture of a core-sheath structure.
  • the device preferably has a spinning plate for the generation of a core-sheath structure, in which the device generates the casing with a polyethylene-containing polymer and the core with a polypropylene-containing polymer.
  • the spinning plate and all the remaining components of the device are adjusted for the procedural parameters necessary in each case for the different polymers. This for instance means that different temperatures, different line diameters and different polymer extruders can be made available.
  • a procedure is made available for the manufacture of a nonwoven fabric the fibers of which have polyethylene on the surface at least in parts, whereby the fibers can be further processed after take-off at a velocity of at least 650 m/min, in particular 1500 m/min from a spinning plate, where the polymer is heated in an extruder to between 200° C. and 250° C. and passed at that temperature through a spinning plate heated to between 190° C. and 240° C., where the polymer is divided into individual polymer threads in a spinning plate with a least over 4500 holes/m, where the polymer threads in each case flow through the spinning plate along a path that is at least four times as long as a polymer thread diameter.
  • the polymer thread diameter used here is the diameter at the exit from the spinning plate.
  • the polymer threads prefferably it is provided for the polymer threads to be stretched at a take-off velocity of 3000-4500 m/min.
  • the polyethylene is preferably mixed as dry blend with another polymer before going into the extruder. This has shown particularly advantageous effects during processing, since thereby the throughput can be increased to over 160 kg/h/m.
  • the polymer thread to be deposited on a screen belt, to be subsequently compacted by means of a calender, the rollers of which are heated to different degrees. Consolidation occurs in a thermal bonding step. It is preferably provided for the polymer threads to be thermally bonded in a temperature range of 112-135° C., with a consolidated area fraction of less than 30%, preferably less than 28%, especially less than 23%.
  • a nip pressure in the calender amounts to 40-80N/mm, particularly to only 40-60 N/mm.
  • a polyethylene being a homo- or a copolymer is bonded in a temperature range that can reach up to 140° C.
  • a Bico material is bonded in a temperature range than can reach up to 155° C.
  • the nonwoven fabric can be used to particular advantage in an application in which it is used on the outside of a product, as covering.
  • the polymer material used for the fibers can be a polyethylene by itself, or in a blend.
  • a blend can be obtained either by compounding or by dry-blending of one or several polymers.
  • the concept “polymer” includes homopolymers, copolymers and inter-polymers, i.e., polymers formed by polymerization of at least two different kinds of monomers. This means that the polymer material can be a copolymer, a terpolymers, etc.
  • the polyethylene polymer can for instance be a LDPE, a LLDPE and/or a HDPE.
  • They can be formed by homopolymerization of ethylene, or by inter-polymerization, for instance copolymerization of ethylene with one or several vinyl or diene-based comonomers.
  • An ⁇ -polyolefin with three to twenty carbon atoms can for instance be used, or a vinyl ester, or a styrene-based monomer, as well as other copolymerization reactions.
  • the polyethylene that can be used can for instance be of homogeneous or inhomogeneous linkage of the molecules.
  • short-chain polyethylene polymers can also be used.
  • LLDPE and HDPE can be used.
  • the polyethylene preferably has a bimodal molecular weight distribution, but the polymer or copolymer, respectively, can also have a unimodal molecular weight distribution.
  • a polyethylene with octene, in particular a metallocene-LLDPE with octene is preferred.
  • polyethylene-containing material can be used by itself or in mixtures with other polymer material in the manufacture of nonwoven fabric fibers which was used to date only in the injection molding area, especially for roto-molding, for sheets or other plastic processing areas, but not in the nonwoven fabric area.
  • a polymer material can for instance include a polyethylene blend by itself, or as a partial constituent, as described in US 2003/0149180. It is also possible to use homo and copolymers and polymer blends, for instance with polypropylene, as described in EP 260 974 A1, for example. Regarding the polymers necessary to manufacture nonwoven fabric fibers, their manufacture and composition, in the framework of this invention it is referred to these two documents, the content of which are part of the disclosure in this description.
  • An essentially linear polyethylene can for instance be manufactured in a continuous process, with at least one reactor. Something of this type is for instance described in WO 93/07187, WO 93/07188 and WO 94/07189, the content of which is part of the description, within the framework of this disclosure.
  • a multiple reactor arrangement can also be used, for instance as described in U.S. Pat No. 3,914,342. The disclosure made there is hereby also included in this description.
  • the polyethylene can for instance be manufactured using a Ziegler-Natta, or a Kaminsky-Sinn polymerization reaction.
  • the polyethylene can be manufactured by a metallocene process.
  • the possibility furthermore exists of manufacturing polymer mixtures by manufacturing each fraction of the mixture separately and combining them only subsequently. This has the advantage of particularly variable regulation possibilities, by changing the individual fractions.
  • Another possibility provides for a reactor to be adjusted for a desired polyethylene-containing polymer, to be then operated continuously at this ratio.
  • a LLDPE that has a density preferably in the range of 0.9-0.955 g/cm 3 .
  • a ULDPE or a VLDPE can for instance be used, with densities in the range of 0.87-0.91 g/cm 3 , approximately.
  • a HDPE with a density of for instance 0.941-0.965 g/cm 3 can be used.
  • PE materials with different densities mixed together can be used.
  • a polyethylene material in which the M w /M N range lies for instance between 2 and 4, in particular between 2.6 and 3.2.
  • the material preferably has a molecular weight in the range of 40,000-55,000 g/mol, in particular of 46,000-52,000 g/mol.
  • the density is preferably adjusted to 0.85-0.955 g/cm 3 .
  • the MFI preferably lies in the range of 10-30 g/10 min at 190° C./2.16 kg. It is in particular also possible to mix two or more polymers, for instance as dry blend or as compound. This material comprises preferably the same parameters as mentioned above.
  • At least one polyethylene-containing polymer has a high MFI, for instance of 30 g/10 min at 190° C./2.16 kg, with a high density, and the second polyethylene has a lower MFI, for instance of 10, and a lower density than the first one.
  • the polymers are preferably unimodal.
  • Another implementation provides for the use of a polyethylene-containing polymer with a density of 0.955 g/cm 3 and an MFI of 29 g/10 min at 190° C./2.16 kg.
  • Another implementation comprises or consists of at least a PE polymer that has a bimodal molecular weight distribution.
  • thermoplastic material can be mixed with the polyethylene material, or arranged next to it.
  • the thermoplastic material can for instance be a polyolefin such as polypropylene, or a polylactitol, an alkenyl-aromatic polymer, a thermoplastic polyurethane, a polycarbonate, a polyamide, a polyether, a polyvinyl chloride and/or a polyester, or other polymer materials such as block polymers and elastomers. This listing is not intended to be limiting.
  • a nonwoven fabric fiber can include other material fractions, for instance additives. They can be added as master batch and/or during compounding. Antioxidants and/or other additives can for instance be used. A property of the nonwoven fabric may thereby be influenced, or also by treating the nonwoven fabric with a fluid, for instance by coating, spraying, diffusion, etc.
  • additives examples include flame retarding additives.
  • stabilizing the nonwoven fabric with respect to solar and other radiation for instance heat, beta and/or gamma rays.
  • thermal and/or UV stabilizers can be used as additives (for instance HALS, hindered amine light stabilizer).
  • opalescent pigments for instance.
  • Colored additives can also be used, for instance in the form of pigments.
  • clarifying agents as additives, and/or nucleating additives, optical brighteners, fragrances such as perfumes, aromatic additives such as spices like vanilla, hydrophilizing agents, hydrophobing agents, fillers, titanium dioxide, and antistatic agents.
  • additives or coatings with antimicrobial effects such as biostatic or biocidal additives, depending on the desired use of the invention.
  • substances with antimicrobial activity are Irgaguard B 1000 from Ciba Specialty Chemicals, or numerous commercially available products that contain silver ions (for instance AlphaSan RC 5000 from Milliken Chemical).
  • Odor-controlling additives such as zeolites can also be added.
  • a polyethylene is for instance used that has a MFI of 15 g/10 min at 190° C./2.16 kg, measured following ISO 1133.
  • the material has a density of 0.935 according to ISO 1183 and a melting point of 127° C.
  • the Vicat softening temperature is 111° C. as measured by ISO 306 (Method A120).
  • the crystallization temperature is 107° C. as measured by DSC.
  • This polyethylene can be spun as homopolymer, or in combination with another polymer material.
  • An additional polyethylene material that can be spun by itself or in a mixture, has a MFI of 27 g/10 min at 190° C./2.16 kg according to ISO 1133.
  • the density is 0.941 g ⁇ cm 3 according to ASTM D-792.
  • the DSC melting temperature is 126° C.
  • Another polyethylene material that can be spun has a MFI of 30 g/10 min at 190° C./2.16 kg, according to ISO 1133.
  • the density is 0.955 g/cm3 per ASTM D-792.
  • the DSC melting temperature is 132° C.
  • These polymers mentioned as examples were spun in some cases as homopolymers and in others as polymer mixtures with other thermoplastic materials, especially with those mentioned. Preferably these and others have molecular weights in the range of 20,000-70,000 g/mol, preferably in a range of 40,000-70,000 g/mol.
  • the polymers can in particular also be processed in the temperature range of 190-240° C. Below other advantageous polymer materials are discussed in greater detail.
  • this polyethylene has for instance proven to be positive to mix different polyethylene materials with each other. This can be realized as a dry blend, but also in an appropriate compounding.
  • this polyethylene has a different density and a different MFI than the at least second polyethylene material. It is particularly advantageous if the MFI of the material to be spun is >20.
  • polyethylene materials can furthermore be provided for various polyethylene materials to be mixed together and then adding one or more additional polymers.
  • Two or more polyethylene materials can for instance be in a mixing ratio in a band width of 80:20 to 20:80.
  • a polypropylene can for instance be added.
  • the polypropylene can for instance be isotactic, or also syndiotactic or atactic. It was shown to be particularly advantageous for the MFI of the material to be spun to be >25, in particular in the range of 28-35 g/10 min according to ASTM D-1238. It was also found to be particularly advantageous for the density of the material to be spun to be in the range of 0.935-0.975 g/cm 3 .
  • a MFI value >20 for the material to be spun preferably a MFI value between 20 and 30.
  • a spinning temperature in a range of for instance 19-225° C.
  • the nip pressure in the downstream calender in a very low range.
  • the calender nip pressure had a value in the range of 40-70 N/mm, in particular of 40-60 N/mm, at the same time achieving a stable embossing result. In particular, this makes possible a durable process able to run for several hours at constant fiber or nonwoven fabric results.
  • the calender has also proven advantageous for the calender to have a roughness R z of approximately 35-50 ⁇ m, in particular of 40 ⁇ m. However, the surface roughness can also be higher or lower. If a coating is applied, for instance, it advantageously has a layer thickness of 100-200 ⁇ m. A polymer coating can for instance be provided for.
  • the polymer material used has a width of molecular weight distribution M W /M N of 2-3.5. It has also proven to be advantageous to add a master batch containing a stabilizer, for some polyethylenes or polyethylene-containing mixtures.
  • the fraction of the master batch can here for instance be of up to 5 wt.-% of the material to be spun. It was preferably established in some tests that an addition of master batch in the range of 0.1-1.5 wt.-%, with the correspondingly lower stabilizer fraction, was sufficient.
  • a fluoro-elastomer can furthermore for instance be added to the polyethylene or the polyethylene copolymer.
  • the fluoro-elastomer contributes to avoid cracking of the spinning plate.
  • Another implementation provides for a lubricant to be added to the polymer material.
  • the lubricant can here be added in a dry blend, or during compounding.
  • the lubricant added can for instances be an internal, or also an external lubricant.
  • the lubricant accomplishes a further reduction in the fiber's titer.
  • Examples of lubricants that can be used are for instance fatty acids, for instance monoamido-fatty acids, carbonated fatty acids and fatty acid mixtures. It is furthermore possible to use polyethylene wax, montan wax and wax emulsions. Hydrocarbon wax in particular has proven advantageous as an internal lubricant.
  • a polyethylene material is used that has an MFI value of 15-20 g/10 min at 190° C./2.16 kg for the material to be spun. This makes it possible to set a temperature at the spinning plate that is in the range for instance of 190-250° C. In particular, it also makes possible setting a nip pressure in the calender downstream that is very low.
  • the calender nip pressure can preferably have a value of 40-60 N/mm.
  • An extruder temperature profile can furthermore be built in such a way that the temperature is higher in the inlet area than in the outlet area.
  • the temperature profile can also be such that the temperature in the inlet area is lower than that in the outlet area.
  • the temperature can for instance first increase and then decrease again.
  • the configuration used to perform some of the spinning tests for the manufacture of two-component fibers was performed on a Reifen Reifenberger III beam.
  • Two separate extruders and spinning pump systems were used.
  • the first extruder has a screw of 150 mm diameter with different screen packs of order of magnitude 60, 180 and 250 mesh (0.16, 0.05 and 0.04 mm).
  • the second extruder has a screw of 80 mm diameter and screen packs of order of magnitude 50 and 120 mesh (0.2 and 0.08 mm).
  • a spinning package with a spinning plate with 5.297 holes (4.414 holes per m) was used. Each hole had a diameter of 0.6 mm and an L/D ratio of 4.
  • the calender had a smooth-faced roller and an engraved roller, both of which were heated.
  • the engraved roller had an oval embossing pattern, where the fraction of embossing area was 16.19%.
  • the land area points were 0.83 ⁇ 0.5 mm with a depth of 0.84 mm.
  • the temperature of each roller could be regulated separately.
  • the nip pressure in the calender could also be adjusted.
  • different consolidating patterns were used in this as in other calenders in other tests. Elliptical, round, diamond-shaped, rod-shaped and U-shaped patterns were used, with consolidated area fractions of 14.5-35%.
  • the extruder was for instance adjusted as follows:
  • the first extruder had an outlet temperature of 210-228° C. at the extruder head.
  • the second extruder was operated in a temperature range of 210-230° C. at the extruder head.
  • the temperature of the second extruder could here differ from that of the first extruder.
  • the temperature difference used for the extruder head was for instance of 5-15° C. Good results were also obtained with Bico materials when the exit temperatures were the same.
  • the temperature of the spinning block was set to 220-240° C.
  • the pressure applied to the spinning block was of 30-50 bar, but it can also be in the range of 70-100 bar.
  • the cabin pressure was varied between 13 and 20 mbar.
  • the quenching was performed at a temperature between 16.5 and 24° C. However, these parameters are only indicated as examples.
  • the cabin pressure for example can have values of up to 50 mbar and beyond.
  • the quenching temperature can also be above or below the range indicated.
  • the spinning plate used had 162 holes of capillary borings with 1.4 mm diameter each.
  • the melt temperature and the spin plate temperature were varied, with especially good results obtained in the range of 205-220° C.
  • Also used for instance was a spin pack equipped with a spinning plate with 105 holes and a capillary diameter of 0.6 mm.
  • the LID ratio was 8.
  • first and the second extruder were also used in the manufacture of nonwoven materials of a single material. This means that a homogeneous material was used. It was possible here to use both extruders simultaneously, or just one of them. When both extruders were used simultaneously, their parameters and in particular, their temperature profiles, were set at least approximately equal. Here the parameters could vary in the same ranges indicated above for the first extruder on the one hand, and for the second on the other.
  • a Lurgi-Docan line was for instance also used to perform these tests. For instance, a spinning package with 2.268 holes/m in the spinning plate was used. Temperatures between 175° C. and 269° C. were set.
  • test results are merely examples and should not be viewed as limiting.
  • Resin A is an ethylene homopolymer having a melt index (l 2 ) of 30 gram/10 minutes and a density of 0.955 g/cc.
  • Resin B is an ethylene homopolymer having a melt index (l 2 ) of 27 gram/10 minutes and a density of 0.941 g/cc.
  • Resin C is a homogeneous substantially linear ethylene/a-olefin having a melt index (l 2 ) of 30 gram/10 minutes and a density of 0.913 g/cc.
  • Resin D is an ethylene/1-octene copolymer, comprising about 40% (by weight) of a substantially linear polyethylene component having a melt index of about 30 g/10 minutes and a density of about 0.915 g/cc and about 60% of a heterogenous Ziegler Natta polyethylene component; the final polymer composition has a melt index of about 30 g/10 minutes and a density of about 0.9364 g/cc.
  • Resin E is an ethylene/1octene copolymer, comprising about 40% (by weight) of a substantially linear polyethylene component having a melt index of about 15 g/10 minutes and a density of about 0.915 g/cc and about 60% of a heterogenous Ziegler Natta polyethylene component; the final polymer composition has a melt index of about 22 g/10 minutes and a density of about 0.9356 g/cc.
  • Resin F is an ethylene/1-octene copolymer, comprising about 40% (by weight) of a substantially linear polyethylene component having a melt index of about 15 g/10 minutes and a density of about 0.915 g/cc and about 60% of a heterogenous Ziegler Natta polyethylene component; the final polymer composition has a melt index of about 30 g/10 minutes and a density of about 0.9367 g/cc.
  • Resin G is an ethylene/1-octene copolymer, comprising about 55% (by weight) of a substantially linear polyethylene component having a melt index of about 15 g/10 minutes and a density of about 0.927 g/cc and about 45% of a heterogenous Ziegler Natta polyethylene component; the final polymer composition has a melt index of about 20 g/10 minutes and a density of about 0.9377 g/cc.
  • Resin H is homopolymer polyproylene having a melt flow rate of 25 g/10 minutes in accordance with ASTM D-1238 condition 230° C./2.16 kg.
  • Resins D, E, F, and G can be made according to U.S. Pat. Nos. 5,844,045, 5,869,575, 6,448,341, the disclosures of which are incorporated herein by reference. Melt index is measured in accordance with ASTM D-1238, condition 190° C./2.16 kg and density is measured in accordance with ASTM D-792.
  • Nonwoven fabric was made using the resins indicated in the table mentioned below and evaluated for spinning and bonding performance.
  • the trials were carried out on a spunbond line which used a Reicofil III technology with a beam width of 1.2 meters. The line was run at an output of 107 kg/hour/meter (0.4 g/min/hole) for all polyethylene resins and 118 kg/hour/meter (0.45 g/min/hole) with the polypropylene resin. Resins were spun to make about 2.5 denier fibers, corresponding to the fiber velocity of about 1500 m/min at 0.4 g/min/hole output rate. A mono spin pack was used in this trial, Each spinneret hole had a diameter of 0.6 mm (600 micron) and a L/D ratio of 4. Polyethylene fibers were spun at a melt temperature of 210° C. to 230° C. and polypropylene fibers were spun at a melt temperature of about 230° C.
  • the embosses roller of the chosen calendar had an oval pattern with a bonding surface of 16.19%, an areas amount/cm 2 of 49.90, a land are width of 0.83 mm ⁇ 0.5 mm and a depth of 0.84 mm.:
  • the embossed calendar and smooth roller were set at the same oil temperature.
  • the smooth roller was set 2° C. lower than the embossed roller (this was to reduce tendency of roller wrap). All calendar temperatures that are mentioned in this report were the oil temperature of the embossed roll.
  • the surface temperatures on the calendars were not measured. The nip pressure was maintained at 70 N/mm for all the resins.
  • the mono or multilayered nonwoven fabric can be additionally consolidated, bonded, laminated and/or mechanically treated, in particular composited with another material. This can for instance be accomplished physically, chemically, frictionally coupled and/or interlocking. For instance, thermal and/or ultrasonic bonding possibilities may be used. An adhesive can also be used.
  • the nonwoven fabric can be included in a SM or SMS material, for instance as known from U.S. Pat. Nos. 5,178,931 and 5,188,885, or with a melt-blown material, as for instance known from U.S. Pat. Nos. 3,704,198 and 3,849,241.
  • Multilayer materials can also be formed, for instance as known from WO 96/19346.
  • two-component materials for instance as they are known from U.S. Pat. Nos. 5,336,552, 5,382,490, 5,759,926 and 5,783,503 and the documents mentioned therein.
  • co-extruded fibers as they are known from U.S. Pat. Nos. 4,100,324 and 4,818,464.
  • the nonwoven fabric can be stretched by itself or bonded to at least one additional layer.
  • the material can exhibit elastic properties.
  • the stretching force can here be applied in CD and/or in MD. Methods and parameters for such stretching can for instance be found in EP 0 259 128 B1, in U.S. Pat. No. 5,296,184, in EP 0 309 073 and in U.S. Pat. No. 5,770,531. It is referred to them in the context of this disclosure in relation to stretch possibilities.
  • nonwoven fabric refers to a web that has a structure of individual fibers or threads which are interlaid, but not in any regular, repeating manner.
  • Nonwoven fabrics can be formed by a variety of processes, such as, for example, air laying processes, meltblowing processes, spunbonding processes and carding processes, including bonded carded web processes.
  • the nonwoven fabric might comprise microfibers.
  • Microfibers refers to small diameter fibers having an average diameter not greater than about 100 microns. Fibers, and in particular, spunbond fibers utilized in the present invention can be microfibers, or more specifically, they can be fibers having an average diameter of about 15-30 microns, and having a denier from about 1.5-3.0.
  • the nonwoven fabric might comprise meltblown fibers.
  • meltblown fibers refers to fibers formed by extruding a molten thermoplastic material through a plurality of fine, usually circular, die capillaries as molten threads or filaments into a high velocity gas (e.g., air) stream which attenuates the filaments of molten thermoplastic material to reduce their diameter, which may be to a microfiber diameter. Thereafter, the meltblown fibers are carried by the high velocity gas stream and are deposited on a collecting surface to form a web of randomly dispersed meltblown fibers.
  • a high velocity gas e.g., air
  • the nonwoven fabric might comprise spunbond fibers, especially consists spun-bond fibers.
  • spunbond fibers refers to small diameter fibers which are formed by extruding a molten thermoplastic material as filaments from a plurality of fine, usually circular, capillaries of a spinneret with the diameter of the extruded filaments then being rapidly reduced by drawing.
  • the nonwoven fabric might be consolidated.
  • the terms “consolidation” and “consolidated” refer to the bringing together of at least a portion of the fibers of the nonwoven fabric into closer proximity to form a site, or sites, which function to increase the resistance of the nonwoven to external forces, e.g., abrasion and tensile forces, as compared to the unconsolidated fabric.
  • Consolidated can refer to the entire nonwoven fabric that has been processed such that at least a portion of the fibers are brought into closer proximity, such as by thermal point bonding. Such a web can be considered a “consolidated web”.
  • a specific, discrete region of fibers that is brought into close proximity, such as an individual thermal bond site can be described as “consolidated”.
  • Consolidation can be achieved by methods that apply heat and/or pressure to the fibrous web, such as thermal spot (i.e., point) bonding.
  • Thermal point bonding can be accomplished by passing the fibrous web through a pressure nip formed by two rolls, one of which is heated and contains a plurality of raised points on its surface, as is described in the aforementioned U.S. Pat. No. 3,855,046 issued to Hansen et al.
  • Consolidation methods can also include ultrasonic bonding, through-air bonding, and hydroentanglement.
  • Hydroentanglement typically involves treatment of the fibrous web with high pressure water jets to consolidate the web via mechanical fiber entanglement (friction) in the region desired to be consolidated, with the sites being formed in the area of fiber entanglement.
  • the fibers can be hydro-entangled as taught in U.S. Pat. Nos. 4,021,284 issued to Kalwaites on May 3, 1977 and 4,024,612 issued to Contrator et al. on May 24, 1977, both of which are hereby incorporated herein by reference.
  • the polymeric fibers of the nonwoven are consolidated by point bonds, sometimes referred to as “partial consolidation” because of the plurality of discrete, spaced-apart bond sites.
  • the nonwoven fabric can be used in the most varied applications, which are here reflected merely as examples, without claim to completeness.
  • the nonwoven fabric can be used in absorbent articles.
  • absorbent article refers to devices which absorb and contain body exudates, and, more specifically, refers to devices which are placed against or in proximity to the body of the wearer to absorb and contain the various exudates discharged from the body.
  • the nonwoven fabric can also be used in disposable articles.
  • dispenser is used herein to describe absorbent articles which are not intended to be laundered or otherwise restored or reused as an absorbent article (i.e., they are intended to be discarded after a single use and, preferably, to be recycled, composted or otherwise disposed of in an environmentally compatible manner).
  • a “unitary” absorbent article refers to absorbent articles which are formed of separate parts united together to form a coordinated entity so that they do not require separate manipulative parts like a separate holder and liner.
  • nonwoven fabric In the medical area, for instance in a Stoma bag, coverings, gowns, face masks, ladies' and babies' hygiene articles, for instance back sheets, or also as top sheets, which for instance may also have a coating, in sanitary towels, incontinence articles, printable coverings, protective surfaces, packaging materials, as separators, as vapor-permeable but water-tight materials, as adhesive material for instance in the use of microloops and locking devices, as fastening material in closure systems, as contact surface for an adhesive, as contact agent between two surfaces, for instance a bed and a bed cover, as part of a wall hanging or carpet or floor material, as cleaning or polishing agent, in protective clothing, for instance an overall, in applications close to the skin.
  • oil and/or lubricant collector and/or as cleaning agent in sport clothes, sport accessories and/or sport equipment, or shoes, in clothing items such as gloves, coats, etc., as packaging, for instance for bottles, CD wrappers, as wrapping, as decoration, in the automobile domain, in the fittings area, as covering material to wrap articles, as a coating, as roofing material, as noise and/or thermal insulation, as filtering agent or sedimentation agent, as identification agent for instance in creme application fabrics, as storage medium for substances that during subsequent use are suddenly or gradually released, for instance by diffusion, as eyeglass cleaning fabric, as loading medium for particles and/or powders, as intermediate layer in hygiene articles, in the sanitary area, for instance in towels, in bathing caps, as drainage agent, as color-coding agent, as signal marker, as seat cover, as wound covering material, in elastic bandages, as cigarette filter, as surface material in a disposable article, as covering material for painting, coating and similar work, to grow cell cultures, in elastic materials, for instance in hygiene articles as sidebands, waste-bands, in
  • FIG. 1 is a schematic view showing a first spinning system that operates according to the Lurgi-Docan process
  • FIG. 2 is a schematic view showing a second device for the manufacture of spunbond nonwoven fabrics
  • FIG. 3 is a top view showing a first spinning plate
  • FIG. 4 is a top view showing a second spinning plate
  • FIG. 5 is a cross-section all view
  • FIG. 6 a cross sectional view of a first product
  • FIG. 7 cross sectional view of a second product
  • FIG. 8 a cross-section through a nonwoven fabric fiber
  • FIGS. 9 , 10 , 11 a cross-section through bicomponent fibers.
  • FIG. 1 shows a first device 1 for the manufacture of nonwoven fabric fibers 2 .
  • polymer sent to the extruder 3 is melted and sent to a spinning package 5 through an extruder head 4 .
  • the extruder head 4 and the spinning package 5 can be heated independently of each other.
  • a spinning plate 6 is included in the spinning package 5 .
  • the polymer 7 coming from the extruder is pressed through the spinning plate 6 .
  • the polymer continues as individual threads, which are cooled and stretched by means of quenching device 8 .
  • the quenching device provides for a quenching medium 9 , indicated by arrows, to cool the polymer threads 10 coming out of the spinning plate 6 .
  • the polymer threads 10 are sent into a gap area 12 .
  • a propelling agent is introduced, for acceleration. In particular this can be driving air.
  • a spreading medium 14 is introduced, to spread the polymer threads 10 in a downstream diffuser area 15 .
  • the nonwoven fabric fibers 16 thus stretched and spread can then be deposited on a device not further shown, for further processing. With the device described and properly chosen parameters it is possible to manufacture a nonwoven fabric as described above.
  • a bonding facility is added downstream of the first device 1 , in particular a calender system, so that the nonwoven fabric can be manufactured in a single process, from polymer melting to processing to nonwoven fabric fibers, to consolidation in a calendering system.
  • FIG. 2 shows a second device 17 , that includes an extruder 18 .
  • the extruder 18 has a first segment 19 , a second segment 20 , a third segment 21 , a fourth segment 22 and a fifth segment 23 .
  • the segments 19 - 23 can each be heated separately.
  • the extruder 18 has a heated extruder head 24 .
  • the melted polymer is sent under temperature control to the spinning package 25 , through the extruder head.
  • the polymer 27 under pressure, is sent to the chamber 28 via the spinning package 25 and through the spinning plate 26 that is part of the spinning package 25 .
  • the chamber 28 has an outlet placed across from the spinning package 25 . This outlet can in particular be in the form of a gap, as illustrated.
  • the gap width 29 is adjustable.
  • the outlet 28 preferably opens into an enclosure 30 that preferably has a diffuser area 31 .
  • the diffuser area 31 allows spreading the nonwoven fabric fibers 32 when they are deposited.
  • a first 33 and a second roller area 34 is arranged.
  • the roller areas 33 , 34 are preferably such that they facilitate improved suctioning off of the quenching medium by the deposition facility 35 .
  • a suction system 37 can be arranged underneath the screen belt 36 of the deposit facility 35 .
  • the suction system 37 can preferably be adjusted to different removal volumes, by changes of the suction mechanism 38 .
  • the deposited nonwoven fabric fibers 32 are next compacted or consolidated in a calender 39 , in particular thermally bonded.
  • the calender 39 has an engraved roller 40 and a smooth-surfaced roller 41 . Between the engraved roller 40 and the smooth-surfaced roller 41 an embossing gap 42 is formed, where its nip pressure can be adjusted.
  • the nonwoven fabric can be spooled on a downstream spooling device 43 and stored or further processed as a spool.
  • FIG. 3 shows a first spinning plate 45 in a schematic view.
  • the borings 46 in the spinning plate 45 are arranged in parallel rows and lines perpendicular to each other. In particular, only the borings, or also the entire spinning plate can have a coating 47 .
  • FIG. 4 shows a second spinning plate 48 in a schematic view.
  • the borings are arranged in a staggered fashion.
  • the distances can be displaced by 50%.
  • the distances can also be different, for instance 1 ⁇ 3, 1 ⁇ 4 or 1 ⁇ 5.
  • FIG. 5 shows a schematic cross-section through as third spinning plate. Different boring geometries that can be used are here shown in simplified form.
  • the L/D ratio can be obtained from the cross-section. If the diameter D changes along the length L, then the mean diameter is determined. It is obtained by adding all partial diameters and multiplying by the corresponding partial lengths and next dividing the result by the overall length L.
  • FIG. 6 shows a cut-out of a first product 51 .
  • the product 51 has a polyethylene nonwoven fabric 52 according to the invention on its surface 53 .
  • the product can for instance be a two-layer material, as shown.
  • the laminate can for instance be a film/nonwoven fabric laminate.
  • FIG. 7 shows a cut-out of a second product 54 .
  • the second product 54 is a SMS material, for instance, the layers of which are thermally bonded to each other.
  • the layers Preferably the layers have not only been bonded to each other but also individually consolidated, in a single process.
  • at least one of the spunbound nonwoven fabric layers is a nonwoven fabric according to the invention, with a polyethylene surface.
  • FIG. 8 shows a cross-section through a nonwoven fabric fiber 55 . It shows a core 56 that preferably contains polypropylene. A surface 57 of the nonwoven fabric fiber has polyethylene at least on parts of it. The polyethylene can cover the entire surface, in particular with changing surface geometry, or cover the core 56 discontinuously, as casing 58 . If there are discontinuities, they can advantageously be equipped with an oxidation layer, for thermal bonding.
  • FIGS. 9 , 10 and 11 each show different cross-sections through a two-component fiber.
  • the two-component fiber offers the advantage of allowing the influencing of desired properties of the nonwoven fabric by the choice of the other polymers, for instance the tensile strength.
  • polyethylene forms the surface, at least partially and in particular, completely.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nonwoven Fabrics (AREA)
  • Multicomponent Fibers (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Artificial Filaments (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)
  • Woven Fabrics (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
US11/425,340 2003-12-20 2006-06-20 Polyethylene-based, soft nonwoven fabric Expired - Lifetime US8420557B2 (en)

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US12/363,912 US20090136606A1 (en) 2003-12-20 2009-02-02 Device for the manufacture of polyethylene-based, soft nonwoven fabric

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DE10360845 2003-12-20
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DE2003160845 DE10360845A1 (de) 2003-12-20 2003-12-20 Weiches Vlies auf Basis von Polyethylen
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11236448B2 (en) 2018-11-30 2022-02-01 The Procter & Gamble Company Methods for producing through-fluid bonded nonwoven webs
US11396720B2 (en) 2018-11-30 2022-07-26 The Procter & Gamble Company Methods of creating soft and lofty nonwoven webs
US12091793B2 (en) 2018-11-30 2024-09-17 The Procter & Gamble Company Methods for through-fluid bonding nonwoven webs

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10360845A1 (de) 2003-12-20 2005-07-21 Corovin Gmbh Weiches Vlies auf Basis von Polyethylen
FR2894834B1 (fr) 2005-12-19 2008-08-29 Paul Boye Technologies Sa Materiau textile composite et article de protection pour application nrbc
DE102006029972A1 (de) * 2006-06-29 2008-01-03 Irema-Filter Gmbh Vorrichtung zur Erzeugung eines Faservlieses im Melt-Blown-Verfahren
DE602006012527D1 (de) * 2006-12-15 2010-04-08 Fare Spa Vorrichtung und Prozess zur Herstellung einer Spinnvliesmatte
EP1972703A1 (en) * 2007-03-22 2008-09-24 Borealis Technology Oy Fibers, tapes or filaments comprising a multimodal polyethylene composition
WO2009058477A1 (en) * 2007-10-31 2009-05-07 Exxonmobil Chemical Patents Inc. Polypropylene spunbond fibers
DE102008005466A1 (de) * 2008-01-21 2009-07-23 Fiberweb Berlin Gmbh Polymermischung
US8623982B2 (en) * 2008-12-01 2014-01-07 Fina Technology, Inc. Polyethylene fibers and processes of forming the same
DE102009006099A1 (de) 2009-01-26 2010-09-30 Fiberweb Corovin Gmbh Polyethylenvlies
TWI385286B (zh) * 2009-08-13 2013-02-11 Taiwan Textile Res Inst 製造不織布的設備
EP2473660B1 (en) * 2009-09-03 2015-11-11 First Quality Nonwovens, Inc. Two-sided hydrophilic/hydrophobic nonwoven and method of manufacturing thereof
EP2335906A1 (en) 2009-12-21 2011-06-22 Trioplast AB Prestretched film
WO2011088106A2 (en) * 2010-01-12 2011-07-21 Fiberweb, Inc. Surface-treated non-woven fabrics
EP2547811B1 (en) * 2010-03-19 2014-04-16 Dow Global Technologies LLC Bicomponent fibers
WO2011144752A2 (en) 2010-05-21 2011-11-24 Fiberweb Corovin Gmbh Extruded polymer product and method for making the same
KR101984351B1 (ko) 2010-12-06 2019-05-30 미쓰이 가가쿠 가부시키가이샤 멜트블로운 부직포, 그의 제조 방법 및 장치
KR20140045323A (ko) 2011-01-12 2014-04-16 엘리콘 텍스타일 게엠베하 운트 코. 카게 방사구 번들
US9408761B2 (en) 2011-03-25 2016-08-09 The Procter & Gamble Company Article with nonwoven web component formed with loft-enhancing calendar bond shapes and patterns
BR112014008021B1 (pt) 2011-10-05 2021-04-27 Dow Global Technologies Llc Fibra bicomponente e pano
RU2608917C2 (ru) * 2011-10-05 2017-01-26 Тейджин Арамид Б.В. Фильера для формования комплексной нити
DE102011117458A1 (de) * 2011-11-02 2013-05-02 Oerlikon Textile Gmbh & Co. Kg Vorrichtung zum Schmelzspinnen und Abkühlen von synthetischen Filamenten
US10245537B2 (en) 2012-05-07 2019-04-02 3M Innovative Properties Company Molded respirator having outer cover web joined to mesh
US9290877B2 (en) 2012-06-13 2016-03-22 Ahlstrom Corporation Method of making glazed nonwoven fabric
USD714560S1 (en) 2012-09-17 2014-10-07 The Procter & Gamble Company Sheet material for an absorbent article
DE102013014920A1 (de) * 2013-07-15 2015-01-15 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen
DE102013014918A1 (de) * 2013-07-15 2015-01-15 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen
DE102013014919A1 (de) * 2013-07-15 2015-01-15 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen
DE102013014917A1 (de) * 2013-07-15 2015-01-15 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen
JP6156999B2 (ja) * 2013-11-07 2017-07-05 花王株式会社 起毛不織布の製造方法
DE112015002324T5 (de) * 2014-06-11 2017-03-23 Fibervisions, L.P. Mischfaserfllter
JP6457757B2 (ja) * 2014-07-28 2019-01-23 旭化成株式会社 メルトブローン不織布
KR101833494B1 (ko) 2014-12-31 2018-03-02 주식회사 휴비스 다층 폴리에틸렌 부직포 및 그 제조방법
EP3090711A1 (en) * 2015-05-06 2016-11-09 Fitesa Germany GmbH Non-woven fabric and process for forming the same
WO2017083850A1 (en) * 2015-11-12 2017-05-18 First Quality Nonwovens, Inc. Nonwoven with improved abrasion resistance and method of making the same
CA3011367C (en) * 2016-01-12 2023-08-08 Georgia-Pacific Nonwovens LLC Nonwoven cleaning substrate
MY184560A (en) * 2016-02-22 2021-04-02 Asahi Chemical Ind Long fiber nonwoven fabric with superior tactile sense
MX2019001220A (es) * 2016-08-02 2019-07-04 Fitesa Germany Gmbh Sistema y proceso para preparar telas no tejidas de acido polilactico.
CN106418907B (zh) * 2016-08-20 2019-05-03 揭阳市亮丰达五金塑胶有限公司 一种制鞋用饰品粘贴装置
JP6608860B2 (ja) * 2017-02-28 2019-11-20 ハビックス株式会社 フェイスマスク用不織布及びその製造方法
CN107460641B (zh) * 2017-08-22 2020-03-03 浙江吉和非织造布有限公司 一种柔性非织造布及其制作方法
CN108158037B (zh) * 2017-12-25 2020-11-17 湖北金叶玉阳化纤有限公司 彩色聚乳酸纤维及制备烟用过滤嘴棒时彩色聚乳酸纤维的调节装置
RU200563U1 (ru) * 2019-08-05 2020-10-29 Ольга Николаевна Буланович Теплоизоляционное изделие
RU200562U1 (ru) * 2019-08-05 2020-10-29 Ольга Николаевна Буланович Теплоизоляционное изделие
KR102320794B1 (ko) * 2020-04-02 2021-11-02 도레이첨단소재 주식회사 부직포, 부직포 적층체, 물품 및 부직포의 제조방법
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CN114622341A (zh) * 2020-12-15 2022-06-14 浙江青昀新材料科技有限公司 一种聚乙烯无纺布及其应用
KR102459529B1 (ko) * 2021-08-13 2022-10-27 (주) 한국노텍 가이드 플레이트를 구비한 멜트블로운 부직포 제조장치

Citations (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734375A (en) 1956-02-14 Apparatus for testing abrasion resistance
US3210451A (en) 1960-12-01 1965-10-05 Celanese Corp Spinnerettes
US3502763A (en) 1962-02-03 1970-03-24 Freudenberg Carl Kg Process of producing non-woven fabric fleece
US3704198A (en) 1969-10-09 1972-11-28 Exxon Research Engineering Co Nonwoven polypropylene mats of increased strip tensile strength
US3792944A (en) 1970-07-20 1974-02-19 Mitsubishi Rayon Co Spinneret for composite spinning
US3802817A (en) 1969-10-01 1974-04-09 Asahi Chemical Ind Apparatus for producing non-woven fleeces
US3817680A (en) 1971-09-30 1974-06-18 Heraeus Gmbh W C Synthetic fiber spinning plate with colummar coating layer
US3849241A (en) 1968-12-23 1974-11-19 Exxon Research Engineering Co Non-woven mats by melt blowing
US3855046A (en) 1970-02-27 1974-12-17 Kimberly Clark Co Pattern bonded continuous filament web
US3914342A (en) 1971-07-13 1975-10-21 Dow Chemical Co Ethylene polymer blend and polymerization process for preparation thereof
US3928920A (en) 1966-05-31 1975-12-30 Vepa Ag Sieve drum device for the bonding and strengthening of felt and similar products
US4021284A (en) 1972-11-13 1977-05-03 Johnson & Johnson Nonwoven fabric and method and apparatus for producing the same
US4024612A (en) 1976-04-02 1977-05-24 E. I. Du Pont De Nemours And Company Process for making an apertured nonwoven fabric
US4100324A (en) 1974-03-26 1978-07-11 Kimberly-Clark Corporation Nonwoven fabric and method of producing same
US4283364A (en) 1977-05-04 1981-08-11 Akzona Incorporated Melt spinning of synthetic yarns
EP0259128A2 (en) 1986-09-01 1988-03-09 Nitto Denko Corporation Composite porous sheet of thermoplastics layers on support
EP0260974A2 (en) 1986-09-19 1988-03-23 The Dow Chemical Company Biconstituent polypropylene/polyethylene fibers
JPS63275767A (ja) 1987-04-25 1988-11-14 ライフェンホイゼル、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング、ウント、コンパニー、マシーネンファブリーク 紡績フリースの製造装置
EP0309073A2 (en) 1987-09-25 1989-03-29 Exxon Chemical Patents Inc. Composite breathable housewrap laminates
US4818464A (en) 1984-08-30 1989-04-04 Kimberly-Clark Corporation Extrusion process using a central air jet
JPH03193958A (ja) 1989-12-21 1991-08-23 Unitika Ltd 不織布及びその製造方法
US5178931A (en) 1990-11-26 1993-01-12 Kimberly-Clark Corporation Three-layer nonwoven laminiferous structure
EP0527489A1 (en) 1991-08-13 1993-02-17 Kuraray Co., Ltd. Polyethylene terephthalate-based meltblown nonwoven fabric and process for producing the same
US5188885A (en) 1989-09-08 1993-02-23 Kimberly-Clark Corporation Nonwoven fabric laminates
WO1993007187A1 (en) 1991-10-03 1993-04-15 Du Pont Canada Inc. Catalyst for ethylene polymerization at high temperatures
WO1993007188A1 (en) 1991-10-03 1993-04-15 Du Pont Canada Inc. Activation of catalyst in ethylene polymerization at high temperatures
US5254299A (en) 1987-10-27 1993-10-19 The Dow Chemical Company Method of improving melt spinning of linear ethylene polymers
US5296184A (en) 1990-02-12 1994-03-22 Clopay Plastic Products Company, Inc. Method of making an ultra soft cloth-like embossed plastic film having post-embossed stretched areas
WO1994007189A1 (en) 1992-09-16 1994-03-31 Fanuc Ltd Method for making animation for nc machining program
US5336552A (en) 1992-08-26 1994-08-09 Kimberly-Clark Corporation Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer
US5382490A (en) 1991-08-30 1995-01-17 Nippon Kayaku Kabushiki Kaisha Electrophotographic toner
WO1996019346A2 (en) 1994-12-20 1996-06-27 Kimberly-Clark Worldwide, Inc. Low gauge films and film/nonwoven laminates
US5616408A (en) 1995-12-22 1997-04-01 Fiberweb North America, Inc. Meltblown polyethylene fabrics and processes of making same
US5759926A (en) 1995-06-07 1998-06-02 Kimberly-Clark Worldwide, Inc. Fine denier fibers and fabrics made therefrom
US5770531A (en) 1996-04-29 1998-06-23 Kimberly--Clark Worldwide, Inc. Mechanical and internal softening for nonwoven web
US5783503A (en) 1996-07-22 1998-07-21 Fiberweb North America, Inc. Meltspun multicomponent thermoplastic continuous filaments, products made therefrom, and methods therefor
US5844045A (en) 1993-01-29 1998-12-01 The Dow Chemical Company Ethylene interpolymerizations
US5869575A (en) 1995-08-02 1999-02-09 The Dow Chemical Company Ethylene interpolymerizations
US5935512A (en) 1996-12-30 1999-08-10 Kimberly-Clark Worldwide, Inc. Nonwoven process and apparatus
EP1039007A1 (en) 1998-10-09 2000-09-27 Mitsui Chemicals, Inc. Polyethylene nonwoven fabric and nonwoven fabric laminate containing the same
US6207602B1 (en) 1994-11-23 2001-03-27 Bba Nonwovens Simpsonville, Inc. Nonwoven fabrics and fabric laminates from multiconstituent polyolefin fibers
US20010051267A1 (en) 1998-12-08 2001-12-13 The Dow Chemical Company. Polypropylene/ethylene polymer fiber having improved bond performance and composition for marking the same
WO2002031245A2 (en) 2000-10-13 2002-04-18 The Procter & Gamble Company Abrasion resistant, soft nonwoven
JP2002138359A (ja) 2000-10-27 2002-05-14 Unitika Ltd ポリエチレン系複合長繊維不織布
US6417121B1 (en) 1994-11-23 2002-07-09 Bba Nonwovens Simpsonville, Inc. Multicomponent fibers and fabrics made using the same
US20020114857A1 (en) 2000-06-21 2002-08-22 Takashi Fujii Melt spinning device
US20020117770A1 (en) 2000-12-22 2002-08-29 Kimberly-Clark Worldwide, Inc. Nonwovens with improved control of filament distribution
US6448341B1 (en) 1993-01-29 2002-09-10 The Dow Chemical Company Ethylene interpolymer blend compositions
US20020132923A1 (en) 1998-05-18 2002-09-19 The Dow Chemical Company Articles having elevated temperature elasticity made from irradiated and crosslinked ethylene polymers and method for making the same
US20020144384A1 (en) 2000-12-11 2002-10-10 The Dow Chemical Company Thermally bonded fabrics and method of making same
US20020148578A1 (en) 2001-03-30 2002-10-17 Ian Reilly Device for applying an embossing to a web of tissue paper and method thereof
US20030149180A1 (en) 2001-08-17 2003-08-07 Dow Global Technologies Inc. Bimodal polyethylene composition and articles made therefrom
US20050164586A1 (en) * 2004-01-26 2005-07-28 Autran Jean-Philippe M. Fibers and nonwovens comprising polyethylene blends and mixtures
US20050165173A1 (en) * 2004-01-26 2005-07-28 Autran Jean-Philippe M. Fibers and nonwovens comprising polypropylene blends and mixtures
WO2005111291A1 (en) 2004-04-30 2005-11-24 Dow Global Technologies Inc. Improved fibers for polyethylene nonwoven fabric
US7179412B1 (en) 2001-01-12 2007-02-20 Hills, Inc. Method and apparatus for producing polymer fibers and fabrics including multiple polymer components in a closed system
EP1790467A1 (en) 2005-11-28 2007-05-30 Tredegar Film Products Corporation Elastic laminates and methods of manufacturing same
US20070173162A1 (en) * 2004-04-30 2007-07-26 Samuel Ethiopia Nonwoven fabric and fibers

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3130449A (en) 1962-05-28 1964-04-28 Allied Chem Coated spinneret and process of coating during spinning
NL6605678A (cs) 1966-04-28 1967-10-30
DE2964229D1 (en) 1978-11-30 1983-01-13 Ici Plc Apparatus for spinning bicomponent filaments
US4406850A (en) 1981-09-24 1983-09-27 Hills Research & Development, Inc. Spin pack and method for producing conjugate fibers
DE3541127A1 (de) * 1985-11-21 1987-05-27 Benecke Gmbh J Verfahren zur herstellung eines vlieses aus endlosfaeden sowie vorrichtung zur durchfuehrung des verfahrens
DE3542660A1 (de) * 1985-12-03 1987-06-04 Freudenberg Carl Fa Verfahren zur herstellung von spinnvliesen mit erhoehter gleichmaessigkeit
DE3850408T2 (de) 1987-10-02 1994-10-06 Basf Corp Vorrichtung und Verfahren zur Herstellung von profilierten Mehrkomponentenfasern.
US5162074A (en) 1987-10-02 1992-11-10 Basf Corporation Method of making plural component fibers
US5482772A (en) * 1992-12-28 1996-01-09 Kimberly-Clark Corporation Polymeric strands including a propylene polymer composition and nonwoven fabric and articles made therewith
DE4312419C2 (de) * 1993-04-16 1996-02-22 Reifenhaeuser Masch Anlage für die Herstellung einer Spinnvliesbahn aus aerodynamischen verstreckten Filamenten aus Kunststoff
CA2105026C (en) * 1993-04-29 2003-12-16 Henry Louis Griesbach Iii Shaped nonwoven fabric and method for making the same
US6169045B1 (en) 1993-11-16 2001-01-02 Kimberly-Clark Worldwide, Inc. Nonwoven filter media
US5540979A (en) * 1994-05-16 1996-07-30 Yahiaoui; Ali Porous non-woven bovine blood-oxalate absorbent structure
CA2136575A1 (en) * 1994-06-03 1995-12-04 Ty J. Stokes Highly crimpable conjugate fibers and nonwoven webs made therefrom
US5756031A (en) 1994-08-12 1998-05-26 Toyobo Co., Ltd. Process for preparing polybenzazole filaments and fiber
US6420285B1 (en) * 1994-11-23 2002-07-16 Bba Nonwovens Simpsonville, Inc. Multicomponent fibers and fabrics made using the same
KR100488381B1 (ko) 1995-08-04 2006-04-21 이.아이,듀우판드네모아앤드캄파니 높은필라멘트번수의미세필라멘트폴리에스테르사의제조방법
US5672415A (en) 1995-11-30 1997-09-30 Kimberly-Clark Worldwide, Inc. Low density microfiber nonwoven fabric
DE19620379C2 (de) 1996-05-21 1998-08-13 Reifenhaeuser Masch Anlage zur kontinuierlichen Herstellung einer Spinnvliesbahn
US6379136B1 (en) * 1999-06-09 2002-04-30 Gerald C. Najour Apparatus for production of sub-denier spunbond nonwovens
JP2001248055A (ja) * 2000-02-29 2001-09-14 Idemitsu Petrochem Co Ltd スパンボンド弾性不織布の製造方法
JP2001303420A (ja) * 2000-04-26 2001-10-31 Mitsui Chemicals Inc 高均一性不織布の製造方法およびその装置
WO2002012604A2 (en) 2000-08-03 2002-02-14 Bba Nonwovens Simpsonville, Inc. Process and system for producing multicomponent spunbonded nonwoven fabrics
US6855422B2 (en) 2000-09-21 2005-02-15 Monte C. Magill Multi-component fibers having enhanced reversible thermal properties and methods of manufacturing thereof
US20020094352A1 (en) 2000-11-14 2002-07-18 Ying Guo Bicomponent filament spin pack used in spunbond production
EP1337703B1 (en) 2000-11-20 2009-01-14 3M Innovative Properties Company Fiber-forming process
US7998384B2 (en) 2001-08-02 2011-08-16 Fiberweb Simpsonville, Inc. Spunbond nonwoven fabrics from reclaimed polymer and the manufacture thereof
DE50211394D1 (de) * 2002-02-28 2008-01-31 Reifenhaeuser Gmbh & Co Kg Anlage zur kontinuierlichen Herstellung einer Spinnvliesbahn
US20030171054A1 (en) * 2002-03-07 2003-09-11 Vishal Bansal Multiple component spunbond web and laminates thereof
DE10360845A1 (de) 2003-12-20 2005-07-21 Corovin Gmbh Weiches Vlies auf Basis von Polyethylen

Patent Citations (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734375A (en) 1956-02-14 Apparatus for testing abrasion resistance
US3210451A (en) 1960-12-01 1965-10-05 Celanese Corp Spinnerettes
US3502763A (en) 1962-02-03 1970-03-24 Freudenberg Carl Kg Process of producing non-woven fabric fleece
US3928920A (en) 1966-05-31 1975-12-30 Vepa Ag Sieve drum device for the bonding and strengthening of felt and similar products
US3849241A (en) 1968-12-23 1974-11-19 Exxon Research Engineering Co Non-woven mats by melt blowing
US3802817A (en) 1969-10-01 1974-04-09 Asahi Chemical Ind Apparatus for producing non-woven fleeces
US3704198A (en) 1969-10-09 1972-11-28 Exxon Research Engineering Co Nonwoven polypropylene mats of increased strip tensile strength
US3855046A (en) 1970-02-27 1974-12-17 Kimberly Clark Co Pattern bonded continuous filament web
US3792944A (en) 1970-07-20 1974-02-19 Mitsubishi Rayon Co Spinneret for composite spinning
US3914342A (en) 1971-07-13 1975-10-21 Dow Chemical Co Ethylene polymer blend and polymerization process for preparation thereof
US3817680A (en) 1971-09-30 1974-06-18 Heraeus Gmbh W C Synthetic fiber spinning plate with colummar coating layer
US4021284A (en) 1972-11-13 1977-05-03 Johnson & Johnson Nonwoven fabric and method and apparatus for producing the same
US4100324A (en) 1974-03-26 1978-07-11 Kimberly-Clark Corporation Nonwoven fabric and method of producing same
US4024612A (en) 1976-04-02 1977-05-24 E. I. Du Pont De Nemours And Company Process for making an apertured nonwoven fabric
US4283364A (en) 1977-05-04 1981-08-11 Akzona Incorporated Melt spinning of synthetic yarns
US4818464A (en) 1984-08-30 1989-04-04 Kimberly-Clark Corporation Extrusion process using a central air jet
EP0259128A2 (en) 1986-09-01 1988-03-09 Nitto Denko Corporation Composite porous sheet of thermoplastics layers on support
EP0260974A2 (en) 1986-09-19 1988-03-23 The Dow Chemical Company Biconstituent polypropylene/polyethylene fibers
JPS63275767A (ja) 1987-04-25 1988-11-14 ライフェンホイゼル、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング、ウント、コンパニー、マシーネンファブリーク 紡績フリースの製造装置
JPH0149819B2 (cs) 1987-04-25 1989-10-26 Raifuenhoizeru Gmbh Unto Co Mas Fab
EP0309073A2 (en) 1987-09-25 1989-03-29 Exxon Chemical Patents Inc. Composite breathable housewrap laminates
US5254299A (en) 1987-10-27 1993-10-19 The Dow Chemical Company Method of improving melt spinning of linear ethylene polymers
US5188885A (en) 1989-09-08 1993-02-23 Kimberly-Clark Corporation Nonwoven fabric laminates
JPH03193958A (ja) 1989-12-21 1991-08-23 Unitika Ltd 不織布及びその製造方法
US5296184A (en) 1990-02-12 1994-03-22 Clopay Plastic Products Company, Inc. Method of making an ultra soft cloth-like embossed plastic film having post-embossed stretched areas
US5178931A (en) 1990-11-26 1993-01-12 Kimberly-Clark Corporation Three-layer nonwoven laminiferous structure
EP0527489A1 (en) 1991-08-13 1993-02-17 Kuraray Co., Ltd. Polyethylene terephthalate-based meltblown nonwoven fabric and process for producing the same
US5382490A (en) 1991-08-30 1995-01-17 Nippon Kayaku Kabushiki Kaisha Electrophotographic toner
WO1993007187A1 (en) 1991-10-03 1993-04-15 Du Pont Canada Inc. Catalyst for ethylene polymerization at high temperatures
WO1993007188A1 (en) 1991-10-03 1993-04-15 Du Pont Canada Inc. Activation of catalyst in ethylene polymerization at high temperatures
US5336552A (en) 1992-08-26 1994-08-09 Kimberly-Clark Corporation Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer
WO1994007189A1 (en) 1992-09-16 1994-03-31 Fanuc Ltd Method for making animation for nc machining program
US5844045A (en) 1993-01-29 1998-12-01 The Dow Chemical Company Ethylene interpolymerizations
US6448341B1 (en) 1993-01-29 2002-09-10 The Dow Chemical Company Ethylene interpolymer blend compositions
US6417121B1 (en) 1994-11-23 2002-07-09 Bba Nonwovens Simpsonville, Inc. Multicomponent fibers and fabrics made using the same
US6207602B1 (en) 1994-11-23 2001-03-27 Bba Nonwovens Simpsonville, Inc. Nonwoven fabrics and fabric laminates from multiconstituent polyolefin fibers
US20010003693A1 (en) 1994-11-23 2001-06-14 Gessner Scott L. Nonwoven fabrics and fabric laminates from multiconstituent polyolefin fibers
WO1996019346A2 (en) 1994-12-20 1996-06-27 Kimberly-Clark Worldwide, Inc. Low gauge films and film/nonwoven laminates
US5759926A (en) 1995-06-07 1998-06-02 Kimberly-Clark Worldwide, Inc. Fine denier fibers and fabrics made therefrom
US5869575A (en) 1995-08-02 1999-02-09 The Dow Chemical Company Ethylene interpolymerizations
US5616408A (en) 1995-12-22 1997-04-01 Fiberweb North America, Inc. Meltblown polyethylene fabrics and processes of making same
US5770531A (en) 1996-04-29 1998-06-23 Kimberly--Clark Worldwide, Inc. Mechanical and internal softening for nonwoven web
US5783503A (en) 1996-07-22 1998-07-21 Fiberweb North America, Inc. Meltspun multicomponent thermoplastic continuous filaments, products made therefrom, and methods therefor
US5935512A (en) 1996-12-30 1999-08-10 Kimberly-Clark Worldwide, Inc. Nonwoven process and apparatus
US20020132923A1 (en) 1998-05-18 2002-09-19 The Dow Chemical Company Articles having elevated temperature elasticity made from irradiated and crosslinked ethylene polymers and method for making the same
EP1039007A1 (en) 1998-10-09 2000-09-27 Mitsui Chemicals, Inc. Polyethylene nonwoven fabric and nonwoven fabric laminate containing the same
US20010051267A1 (en) 1998-12-08 2001-12-13 The Dow Chemical Company. Polypropylene/ethylene polymer fiber having improved bond performance and composition for marking the same
US20020019490A1 (en) 1998-12-08 2002-02-14 The Dow Chemical Company Polypropylene/ethylene polymer fiber having improved bond performance and composition for making the same
JP2003519296A (ja) 1999-12-30 2003-06-17 ビービーエイ・ノンウォーヴンズ・シンプソンヴィル，インコーポレイテッド 多成分繊維及びそれを使用して製造される布
US20020114857A1 (en) 2000-06-21 2002-08-22 Takashi Fujii Melt spinning device
WO2002031245A2 (en) 2000-10-13 2002-04-18 The Procter & Gamble Company Abrasion resistant, soft nonwoven
US20020119720A1 (en) * 2000-10-13 2002-08-29 Arora Kelyn Anne Abrasion resistant, soft nonwoven
JP2002138359A (ja) 2000-10-27 2002-05-14 Unitika Ltd ポリエチレン系複合長繊維不織布
US20020144384A1 (en) 2000-12-11 2002-10-10 The Dow Chemical Company Thermally bonded fabrics and method of making same
US20020117770A1 (en) 2000-12-22 2002-08-29 Kimberly-Clark Worldwide, Inc. Nonwovens with improved control of filament distribution
US7179412B1 (en) 2001-01-12 2007-02-20 Hills, Inc. Method and apparatus for producing polymer fibers and fabrics including multiple polymer components in a closed system
US20020148578A1 (en) 2001-03-30 2002-10-17 Ian Reilly Device for applying an embossing to a web of tissue paper and method thereof
US20030149180A1 (en) 2001-08-17 2003-08-07 Dow Global Technologies Inc. Bimodal polyethylene composition and articles made therefrom
US20050165173A1 (en) * 2004-01-26 2005-07-28 Autran Jean-Philippe M. Fibers and nonwovens comprising polypropylene blends and mixtures
US20050164586A1 (en) * 2004-01-26 2005-07-28 Autran Jean-Philippe M. Fibers and nonwovens comprising polyethylene blends and mixtures
WO2005111291A1 (en) 2004-04-30 2005-11-24 Dow Global Technologies Inc. Improved fibers for polyethylene nonwoven fabric
US20070173162A1 (en) * 2004-04-30 2007-07-26 Samuel Ethiopia Nonwoven fabric and fibers
EP1790467A1 (en) 2005-11-28 2007-05-30 Tredegar Film Products Corporation Elastic laminates and methods of manufacturing same

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
International Search Report for PCT/EP2004/004640 filed Apr. 30, 2004.
Office Action for Japanese Application No. 2006-544225 dated Sep. 2, 2010.
Office Action for U.S. Appl. No. 12/363,912, mailed Apr. 1, 2011; 16 pages.
Office Action for U.S. Appl. No. 12/363,922 dated Aug. 19, 2011.
Office Action for U.S. Appl. No. 12/363,922 dated Mar. 19, 2012.
Office Action for U.S. Appl. No. 12/363,922, mailed Apr. 14, 2011; 10 pages.

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11236448B2 (en) 2018-11-30 2022-02-01 The Procter & Gamble Company Methods for producing through-fluid bonded nonwoven webs
US11396720B2 (en) 2018-11-30 2022-07-26 The Procter & Gamble Company Methods of creating soft and lofty nonwoven webs
US11686026B2 (en) 2018-11-30 2023-06-27 The Procter & Gamble Company Methods for producing through-fluid bonded nonwoven webs
US11767622B2 (en) 2018-11-30 2023-09-26 The Procter & Gamble Company Methods of creating soft and lofty nonwoven webs
US12091793B2 (en) 2018-11-30 2024-09-17 The Procter & Gamble Company Methods for through-fluid bonding nonwoven webs

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